[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Gaziler Physical Medicine and Rehabilitation Education and Research Hospital\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":200},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,41,64,92,125,151,177],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100637408","sensorimotor-training-with-a-mobilized-balance-platform-in-patients-with-chronic-low-back-pain-100637408",false,"NCT07603609","Sensorimotor Training With a Mobilized Balance Platform in Patients With Chronic Low Back Pain","Effects of a Sensorimotor Training Protocol Using a Mobilized Balance Platform on Proprioceptive System, Movement Control, and Quality of Life in Patients With Chronic Low Back Pain","Inclusion Criteria:\n\n* Individuals aged between 18 and 55 years\n* Presence of chronic low back pain lasting at least 3 months\n* Pain intensity score of 3 or higher on the Visual Analog Scale (VAS)\n* Individuals with sufficient cognitive ability to understand and follow study procedures\n* Willingness to participate voluntarily in the study\n\nExclusion Criteria:\n\n* Participation in a similar training program within the last 12 months\n* History of lower extremity or spinal surgery\n* Presence of non-mechanical low back pain, inflammatory disease, or tumor\n* Uncontrolled hypertension or cardiac disease\n* History of malignancy\n* Presence of radicular symptoms associated with low back pain\n* Progressive neurological deficits\n* Neurogenic claudication","ALL","18 Years","55 Years",{"count":20,"type":21},44,"ESTIMATED","INTERVENTIONAL",[24],"NA","This randomized controlled study aims to investigate the effects of a sensorimotor training protocol using a mobilized balance platform device on proprioceptive system function, movement control, balance, physical performance, pain severity, and quality of life in patients with chronic low back pain. A total of 44 patients with chronic low back pain will be recruited from the outpatient clinic of Gaziler Physical Medicine and Rehabilitation Training and Research Hospital.\n\nParticipants will be randomly assigned to either a sensorimotor training group or a control group. The intervention group will receive sensorimotor training using the Huber 360 balance system, while the control group will perform a home exercise program including stretching, spinal mobility, lumbopelvic control, and balance exercises.\n\nPain severity, proprioception, functional status, balance, physical performance, and quality of life will be assessed before and after treatment by an assessor blinded to group allocation.",[27],"Low Back Pain","RECRUITING","2026-05-16",{"date":31,"type":32},"2026-05-22","ACTUAL",{"date":34,"type":32},"2026-05-04",{"date":36,"type":21},"2026-11-30",{"name":38,"class":39},"Gaziler Physical Medicine and Rehabilitation Education and Research Hospital","OTHER",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":16,"minAge":48,"maxAge":49,"enrollmentInfo":50,"targetDuration":4,"studyType":22,"phases":52,"briefSummary":53,"conditions":54,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":61,"leadSponsor":63,"locationsCount":40},"100638081","effects-of-mobilized-balance-platform-exercises-on-balance-parameters-in-patients-with-knee-osteoarthritis-100638081","NCT07575425","Effects of Mobilized Balance Platform Exercises on Balance Parameters in Patients With Knee Osteoarthritis","Effects of Mobilized Balance Platform Exercises on Balance Parameters, Functional Status, and Pain in Patients With Knee Osteoarthritis: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Patients aged between 45 and 65 years\n* Diagnosis of knee osteoarthritis classified as Kellgren-Lawrence grade 2 or 3\n* Willingness to participate voluntarily in the study\n\nExclusion Criteria:\n\n* Presence of orthopedic knee implants\n* Kellgren-Lawrence grade 1 or grade 4 knee osteoarthritis\n* Sensory impairment\n* Diagnosis of malignancy\n* Unhealed fractures\n* Circulatory disorders\n* Infection around the knee joint\n* Severe hearing loss or visual impairment\n* Cognitive impairment\n* Uncontrolled hypertension or diabetes mellitus\n* Vestibular disorders causing balance problems, such as vertigo\n* Use of walking assistive devices such as canes or walkers","45 Years","65 Years",{"count":51,"type":21},36,[24],"This prospective single-blind randomized controlled study aims to investigate the effects of mobilized balance platform exercises on balance parameters, pain, functional status, fear of falling, and kinesiophobia in patients with knee osteoarthritis. A total of 36 patients diagnosed with knee osteoarthritis will be recruited from the outpatient clinic of Gaziler Physical Medicine and Rehabilitation Training and Research Hospital.\n\nParticipants will be randomly assigned to one of two groups. The control group will receive conventional physical therapy including transcutaneous electrical nerve stimulation (TENS) and a home exercise program consisting of knee strengthening, balance, range of motion, proprioceptive, and stretching exercises. The intervention group will receive the same conventional treatment in addition to mobilized balance platform exercises using the Huber 360 system.\n\nPain severity, functional status, balance parameters, fear of falling, and kinesiophobia will be evaluated before and after treatment by an assessor blinded to treatment allocation.",[55,56],"Osteearthritis","Knee Arthritis, Osteoarthritis","2026-05-03",{"date":59,"type":32},"2026-05-08",{"date":34,"type":32},{"date":62,"type":21},"2026-10-30",{"name":38,"class":39},{"id":65,"slug":66,"hasResults":11,"nctId":67,"briefTitle":68,"officialTitle":69,"acronym":4,"eligibilityCriteria":70,"healthyVolunteers":11,"sex":16,"minAge":48,"maxAge":71,"enrollmentInfo":72,"targetDuration":4,"studyType":22,"phases":74,"briefSummary":75,"conditions":76,"keywords":81,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":40},"100635252","body-weight-supported-and-virtual-reality-gait-training-in-stroke-patients-100635252","NCT07550270","Body Weight-Supported and Virtual Reality Gait Training in Stroke Patients","A Comparative Evaluation of the Effectiveness of Body Weight-Supported Forward and Backward Gait Training Versus Virtual Reality-Assisted Gait Training in Patients With Stroke","Inclusion Criteria:\n\n* Patients experiencing their first-ever stroke\n* Patients with a post-stroke duration of more than 2 weeks\n* Patients with plantar flexor muscle spasticity of the lower extremity less than grade 3 according to the Modified Ashworth Scale (MAS)\n* Patients with a Brunnstrom stage of the lower extremity greater than 2\n* Patients who are able to stand independently or under supervision for at least 2 minutes for standing assessments\n* Patients who are able to walk at least 10 meters independently or under supervision, with or without an assistive device, for walking assessments\n* Patients with sufficient cognitive function to understand study instructions (Mini-Mental State Examination \\[MMSE\\] score \\> 23)\n* Patients with stable medical and psychological conditions\n* Patients who are willing to participate in the study\n\nExclusion Criteria:\n\n* Patients with bilateral hemispheric lesions\n* Patients with severe cardiovascular or musculoskeletal conditions that prevent walking (e.g., fixed ankle contracture)\n* Patients using a permanent urinary catheter, or those with pressure ulcers or urinary and\u002For fecal incontinence\n* Patients with unilateral neglect\n* Patients with neurological conditions other than stroke that may affect balance performance (e.g., Parkinson's disease, epilepsy, meningitis, cerebellar disorders, vertigo, dizziness, polyneuropathy) or musculoskeletal disorders (e.g., severe low back pain, knee disorders)\n* Patients with severe visual, hearing, or speech impairments","75 Years",{"count":73,"type":21},30,[24],"The aim of this study is to compare the effects of body weight-supported gait training that includes virtual reality-assisted dual-task applications with body weight-supported forward and backward gait training on functional capacity, gait parameters (such as step length, gait speed, and balance), cognitive functions and psychological status in patients with stroke. The findings of this study are expected to contribute to the development of more effective rehabilitation strategies for improving mobility in patients with stroke",[77,78,79,80],"Stroke","Walking Impairment","Balance","Gait Training",[82,83],"stroke","gait training","2026-04-19",{"date":86,"type":32},"2026-04-24",{"date":88,"type":32},"2026-03-26",{"date":90,"type":21},"2026-12",{"name":38,"class":39},{"id":93,"slug":94,"hasResults":11,"nctId":95,"briefTitle":96,"officialTitle":97,"acronym":98,"eligibilityCriteria":99,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":49,"enrollmentInfo":100,"targetDuration":4,"studyType":22,"phases":102,"briefSummary":103,"conditions":104,"keywords":109,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":116,"lastUpdatePostDateStruct":117,"startDateStruct":119,"completionDateStruct":121,"leadSponsor":123,"locationsCount":124},"100629274","impact-of-virtual-reality-vr-based-exercises-on-lower-limb-lymphedema-outcomes-lelo-100629274","NCT07472543","Impact of Virtual Reality (VR) Based Exercises on Lower Limb Lymphedema Outcomes (LELO)","The Effect of Virtual Reality-Assisted Exercises on Gait Parameters, Function, Quality of Life, and Edema Level in Patients With Lower Extremity Lymphedema","VR-LELO","Inclusion Criteria:\n\n* Age between 18 and 65 years\n* Diagnosis of unilateral lower extremity lymphedema following gynecological and\u002For oncological surgery\n* Stage 2 or 3 lymphedema\n\nExclusion Criteria:\n\n* Decompensated heart, lung, or kidney failure\n* Uncontrolled hypertension\n* Presence of systemic infection\n* Local infections in the lower extremity such as erysipelas or cellulitis\n* Venous insufficiency (e.g., deep vein thrombosis)\n* Any neuromuscular or orthopedic disease affecting lower extremity walking\n* Presence of balance disorders\n* Bilateral lymphedema\n* Presence of lipolymphedema\n* Fracture in the lower extremity\n* Active metastasis\n* Speech or language problems\n* Pregnancy\n* Inability to continue treatment (5 days a week for a total of 4 weeks)",{"count":101,"type":21},40,[24],"This randomized controlled study aims to investigate the effects of virtual reality (VR)-assisted gait training, in addition to Complex Decongestive Therapy (CDT), on gait parameters, physical function, quality of life, and edema levels in patients with lower extremity lymphedema. Lymphedema is a progressive condition characterized by the accumulation of protein-rich fluid due to lymphatic drainage insufficiency, leading to chronic inflammation and fibrosis. It impairs gait patterns and reduces functional mobility. VR technologies, such as the RehaWalk system, provide interactive, personalized rehabilitation environments that enhance motor learning, motivation, and adherence to treatment. The study evaluates spatiotemporal gait parameters, three-zone foot analysis (heel, midfoot, forefoot), limb circumferences, ultrasound measurements (dermis, epidermis, subcutaneous fat thickness), and patient-reported outcomes. VR-based training offers a novel, engaging approach to improve physical rehabilitation outcomes in patients with lower limb lymphedema. No significant risks are expected in this study.",[105,106,107,108],"Lymphedema","Gait Dysfunction","Physical Rehabilitation","Chronic Edema",[110,111,112,113,114,115],"lymphedema","virtual reality exercises","ultrasonography","Gait Analysis","Spatiotemporal Parameters","Complex Decongestive Therapy (CDT)","2026-03-13",{"date":118,"type":32},"2026-03-16",{"date":120,"type":32},"2025-09-01",{"date":122,"type":21},"2026-10-01",{"name":38,"class":39},2,{"id":126,"slug":127,"hasResults":11,"nctId":128,"briefTitle":129,"officialTitle":129,"acronym":4,"eligibilityCriteria":130,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":49,"enrollmentInfo":131,"targetDuration":4,"studyType":133,"phases":4,"briefSummary":134,"conditions":135,"keywords":138,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":143,"lastUpdatePostDateStruct":144,"startDateStruct":146,"completionDateStruct":148,"leadSponsor":150,"locationsCount":40},"100568707","comparison-of-standard-myoelectric-hand-and-bionic-hand-use-in-individuals-with-upper-limb-amputation-100568707","NCT06684730","Comparison of Standard Myoelectric Hand and Bionic Hand Use in Individuals With Upper Limb Amputation","Inclusion Criteria:\n\n* Having a transradial amputation or wrist disarticulation due to acquired or congenital causes,\n* Using a standard myoelectric or bionic hand prosthesis for at least 6 months,\n* Being between the ages of 18 and 65,\n* Having no neurological or cognitive disorders, rheumatic diseases, or other upper extremity dysfunction that could affect test results, and\n* Having signed an informed consent form indicating the patient's willingness to participate in the study.\n\nExclusion Criteria:\n\n* Individuals younger than 18 or older than 65,\n* Those with additional musculoskeletal or neurological conditions preventing them from completing the tests and scales,\n* Those with psychiatric disorders or cognitive impairments preventing them from completing the questionnaire and assessment scales,\n* Those with stump or upper extremity conditions preventing them from using their prosthesis.",{"count":132,"type":21},22,"OBSERVATIONAL","This single-center, prospective, comparative study aims to compare hand function, quality of life, patient satisfaction, task completion time, fatigue, and compensatory elbow, shoulder, and cervical movements in individuals with transradial amputation or wrist disarticulation who use either standard myoelectric or bionic hand prostheses. The primary research questions are:\n\n1. Are there differences in patient satisfaction, quality of life, and hand function between individuals using standard myoelectric and bionic hand prostheses?\n2. Do individuals using standard myoelectric and bionic hand prostheses exhibit different kinematics in terms of compensatory shoulder, elbow, and neck movements? Could bionic hand prostheses with their diverse grasping capabilities lead to fewer compensatory movements compared to standard myoelectric hand prostheses?\n3. Can fatigue induced by performing specific activities of daily living alter hand function and upper extremity-neck kinematics in individuals using either standard myoelectric or bionic hand prostheses?\n4. Can cognitive and physical fatigue following activities of daily living lead to different levels of changes in hand function and upper extremity-neck kinematics in individuals using standard myoelectric and bionic hand prostheses?",[136,137],"Transradial Amputation","Wrist Disarticulation",[139,136,140,141,142],"Standard Myoelectric Hand","Bionic Hand","Wrist disarticulation","Amputation of upper limb","2026-02-13",{"date":145,"type":32},"2026-02-17",{"date":147,"type":32},"2024-11-27",{"date":149,"type":21},"2026-04-29",{"name":38,"class":39},{"id":152,"slug":153,"hasResults":11,"nctId":154,"briefTitle":155,"officialTitle":156,"acronym":157,"eligibilityCriteria":158,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":159,"targetDuration":4,"studyType":22,"phases":161,"briefSummary":162,"conditions":163,"keywords":165,"overallStatus":168,"whyStopped":4,"lastUpdateSubmitDate":169,"lastUpdatePostDateStruct":170,"startDateStruct":172,"completionDateStruct":174,"leadSponsor":176,"locationsCount":4},"100608910","whatsapp-based-education-program-for-stroke-patients-100608910","NCT07207694","WhatsApp-Based Education Program for Stroke Patients","The Effect of WhatsApp-Supported Education and Counseling on Healthy Lifestyle Behaviors, Glycemic Control, and Knowledge Levels in Patients With Stroke","WEPS-P","Inclusion Criteria:\n\n* Adults aged 18 years and older\n* Diagnosis of ischemic stroke\n* Mini-Mental Test (MMT) score \\> 18\n* Receiving insulin therapy for type 2 diabetes mellitus (T2DM)\n* Ability to use WhatsApp on a smartphone (participant or caregiver)\n* Willingness to provide informed consent\n\nExclusion Criteria:\n\n* Presence of major organ failure\n* Development of severe T2DM-related complications (e.g., diabetic foot, nephropathy, cardiovascular disease)\n* Cognitive or communication impairments preventing participation",{"count":160,"type":21},84,[24],"Stroke is one of the leading causes of death and disability worldwide, with type 2 diabetes mellitus (T2DM) being a major risk factor that doubles the risk of ischemic stroke. Glycemic dysregulation is observed in nearly two-thirds of patients after acute stroke and is associated with both the severity of the initial cerebrovascular event and the risk of recurrence. Effective glycemic control, patient education, and adherence to treatment are therefore critical for secondary stroke prevention and improved patient outcomes.\n\nMobile health technologies, particularly social media applications, have become increasingly important in supporting chronic disease management. WhatsApp-based education has been shown to improve self-efficacy, self-management, and diabetes knowledge in patients with T2DM. However, there is a limited number of studies investigating the effect of WhatsApp-supported education and counseling on stroke patients with T2DM, especially regarding healthy lifestyle behaviors, glycemic control, and disease-related knowledge.\n\nThis randomized controlled trial aims to evaluate the effect of WhatsApp-supported education and counseling on healthy lifestyle behaviors, glycemic control, and knowledge levels among stroke patients receiving insulin therapy. Participants will be randomly assigned to either the intervention group or the control group. The control group will receive routine face-to-face diabetes education and insulin injection training during hospitalization. The intervention group will receive the same routine education plus a structured WhatsApp-based diabetes education program over four weeks. Educational content will include videos, photos, and booklets focusing on diabetes definition and symptoms, complications, hypoglycemia and hyperglycemia management, foot care, nutrition, exercise, oral antidiabetic and insulin therapy, and insulin injection demonstration. Participants' questions will be answered through WhatsApp messages, supporting continuous learning and adherence after discharge.\n\nA total of 84 participants (42 per group) will be included, based on power analysis with a 5% significance level, 95% power, and accounting for a 10% dropout rate. Randomization will be conducted using block randomization with six combinations via an independent researcher through an online randomization tool. Data will be collected at baseline (T0) and six months after the intervention (T1). The primary outcomes include diabetes knowledge measured by the Revised Diabetes Knowledge Test-2, healthy lifestyle behaviors assessed using the Healthy Lifestyle Behavior Scale, and glycemic control parameters (fasting glucose, fasting insulin, HbA1c, and HOMA-IR).\n\nAll assessments will be performed by a trained nurse in the stroke clinic. Data analysis will include descriptive statistics, parametric or non-parametric tests depending on distribution, and reliability analyses using Cronbach's alpha. Ethical approval has been obtained from the Ethics Committee of SBÜ Gaziler Physical Training and Rehabilitation Research Hospital (Approval No: E-34215015).\n\nThis study is expected to demonstrate that WhatsApp-supported education and counseling improve patient knowledge, promote healthy lifestyle behaviors, and enhance glycemic control in stroke patients with T2DM. These findings may support the integration of digital counseling interventions into rehabilitation programs for secondary prevention and long-term disease management.",[164,77],"Type 2 Diabetes Mellitus (T2DM)",[166,167,82],"Healthy Lifestyle Behaviors","type 2 diabetes mellitus","NOT_YET_RECRUITING","2025-10-02",{"date":171,"type":32},"2025-10-06",{"date":173,"type":21},"2025-10-15",{"date":175,"type":21},"2026-11-15",{"name":38,"class":39},{"id":178,"slug":179,"hasResults":11,"nctId":180,"briefTitle":181,"officialTitle":182,"acronym":4,"eligibilityCriteria":183,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":184,"enrollmentInfo":185,"targetDuration":4,"studyType":22,"phases":186,"briefSummary":187,"conditions":188,"keywords":190,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":192,"lastUpdatePostDateStruct":193,"startDateStruct":195,"completionDateStruct":197,"leadSponsor":199,"locationsCount":40},"100593549","effect-of-transauricular-vagal-stimulation-on-cardiac-function-after-spinal-cord-injury-100593549","NCT07007884","Effect of Transauricular Vagal Stimulation on Cardiac Function After Spinal Cord Injury","The Effect of Transauricular Vagal Nerve Stimulation (taVNS) on Cardiac Autonomic Functions in Patients With Spinal Cord Injury","Inclusion Criteria:\n\n1. Aged between 18-60\n2. Having a traumatic spinal cord injury\n3. Cervical spinal cord injury patients with a history of autonomic dysreflexia\n4. At least 6 months after the injury\n5. Signing an informed consent form showing consent to participate in the study\n\nExclusion Criteria:\n\n1. Having a cardiac or neural pacemaker\n2. Presence of pregnancy\n3. Clinical coronary artery disease confirmed by invasive or coronary computed tomographic angiography\n4. History of acute coronary syndrome (unstable angina, myocardial infarction)\n5. Documented arrhythmia and\u002For use of antiarrhythmic drugs on ECG\n6. Diagnosis of hypertension and use of antihypertensive drugs\n7. Damaged skin lesion in the application area","60 Years",{"count":73,"type":21},[24],"The aim of this study is to investigate the effect of transauricular vagal nerve stimulation (taVNS) on cardiac autonomic functions in patients with spinal cord injury (SCI).",[189],"Spinal Cord Injury (SCI)",[191],"vagus nerve stimülation","2025-06-03",{"date":194,"type":32},"2025-06-06",{"date":196,"type":32},"2024-03-20",{"date":198,"type":21},"2025-09-30",{"name":38,"class":39},""]